scholarly journals Magnetite–Corrole Hybrid Nanoparticles

2018 ◽  
Vol 4 (3) ◽  
pp. 37
Author(s):  
Rute Pereira ◽  
Tito Trindade ◽  
Joana Barata

This study describes the first example of a hybrid material comprising corrole- and silica-coated magnetite nanoparticles. Firstly, cuboid and spheroid magnetite nanoparticles were prepared using a simple hydrothermal route, followed by a silica coating. The hybrid nanoparticles were obtained by promoting a covalent link between a gallium (III)(pyridine) complex of 5,10,15-tris(pentafluorophenyl)corrole (GaPFC) and the surface of magnetite–silica core/shell nanoparticles (Fe3O4@SiO2), shaped both as cuboids and spheroids. The hybrids were characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), ultraviolet-visible spectrophotometry (UV-Vis) and transmission electron microscopy (TEM). Preliminary studies on the capacity of singlet oxygen generation of the hybrid nanoparticles showed that these have lower efficiency values when compared to the pure corrole compound.

2011 ◽  
Vol 306-307 ◽  
pp. 410-415
Author(s):  
Li Sun ◽  
Fu Tian Liu ◽  
Qi Hui Jiang ◽  
Xiu Xiu Chen ◽  
Ping Yang

Core/shell type nanoparticles with an average diameter of 20nm were synthesized by chemical precipitation method. Firstly, Monodisperse Fe3O4 nanoparticles were synthesized by solvethermal method. FeSO4ž7H2O and NaBH4 were respectively dissolved in distilled water, then moderated Fe3O4 particles and surfactant(PVP) were ultrasonic dispersed into the FeSO4ž7H2O solution. The resulting solution was stirred 2 h at room temperature. Fe could be deposited on the surface of monodispersed Fe3O4 nanoparticles to form core-shell particles. The particles were characterized by using various experimental techniques, such as transmission electron microscopy (TEM), X-ray diffraction (XRD), AGM and DTA. The results suggest that the saturation magnetization of the nanocomposites is 100 emu/g. The composition of the samples show monodisperse and the sides of the core/shell nanoparticles are 20-30nm. It is noted that the formation of Fe3O4/Fe nanocomposites magnetite nanoparticles possess superparamagnetic property.


2018 ◽  
Vol 8 (3) ◽  
pp. 411 ◽  
Author(s):  
Mehrdad Khatami ◽  
Hajar Alijani ◽  
Meysam Nejad ◽  
Rajender Varma

Among an array of hybrid nanoparticles, core-shell nanoparticles comprise of two or more materials, such as metals and biomolecules, wherein one of them forms the core at the center, while the other material/materials that were located around the central core develops a shell. Core-shell nanostructures are useful entities with high thermal and chemical stability, lower toxicity, greater solubility, and higher permeability to specific target cells. Plant or natural products-mediated synthesis of nanostructures refers to the use of plants or its extracts for the synthesis of nanostructures, an emerging field of sustainable nanotechnology. Various physiochemical and greener methods have been advanced for the synthesis of nanostructures, in contrast to conventional approaches that require the use of synthetic compounds for the assembly of nanostructures. Although several biological resources have been exploited for the synthesis of core-shell nanoparticles, but plant-based materials appear to be the ideal candidates for large-scale green synthesis of core-shell nanoparticles. This review summarizes the known strategies for the greener production of core-shell nanoparticles using plants extract or their derivatives and highlights their salient attributes, such as low costs, the lack of dependence on the use of any toxic materials, and the environmental friendliness for the sustainable assembly of stabile nanostructures.


2019 ◽  
Vol 39 (3) ◽  
pp. 271-278 ◽  
Author(s):  
Suruchi Suri ◽  
Mohd. Aamir Mirza ◽  
Md. Khalid Anwer ◽  
Abdullah S. Alshetaili ◽  
Saad M. Alshahrani ◽  
...  

Abstract The aim of the current study was to develop a dual-loaded core shell nanoparticles encapsulating paclitaxel (PTX) and ellagic acid (EA) by membrane dialysis method. Based on particle size, polydispersity index (PDI), and entrapment efficiency, the dual drug-loaded nanoparticles (F2) was optimized. The optimized nanoparticles (F2) showed a particle size of 140±2 nm and a PDI of 0.23±3. The size and the morphology were confirmed by transmission electron microscopy (TEM) and found agreement with the results of dynamic light scattering. The entrapment efficiencies of total drug (PTX and EA), PTX, and EA in the nanoparticles (F2) were measured as 80%, 62.3%, and 37.7%, respectively. The in vitro release profile showed a controlled release pattern for 48 h. A higher cytotoxicity was observed with nanoparticles (F2) in comparison to free PTX. The results revealed that co-delivery of PTX and EA could be used for its oral delivery for the effective treatment of breast cancer.


2013 ◽  
Vol 274 ◽  
pp. 432-435
Author(s):  
Hong Xia Shen ◽  
Zheng Zhi Yin ◽  
Qiong Cheng

Superparamagnetic core/shell nanoparticles have been prepared successfully by the reduction of Au3+ onto the surface of superparamagnetic nanoparticles. The core/shell nanoparticles were characterized by Transmission electron microscopy (TEM), X-ray powder diffraction patterns (XRD), UV–vis spectrophotometer, Vibration Sample Magnetometer(VSM) and micro-confocal Raman system. The results revealed that the prepared core/shell nanoparticles were covered by Au shell. These superparamagnetic nanoparticles can be highly sensitively detected and afford new opportunities for biomedical applications through chemical bonding of bioactive molecules with the Au shell of nanoparticles.


NANO ◽  
2016 ◽  
Vol 11 (09) ◽  
pp. 1650103 ◽  
Author(s):  
Xiaoman Wang ◽  
Junda Song ◽  
Hongling Chen

In this paper, we prepared the rattle type nanoparticles ZnO@void@SiO2 by two successive coating processes, followed by heat treatment. The carbon layer was formed over ZnO surface with the aid of the hydrothermal treatment of glucose. Then the resulting composite was used to fabricate a silica shell on the surface by sol–gel method. Finally, ZnO particles were released but still trapped inside the silica hollow after calcination, that is, ZnO@void@SiO2. The composites were characterized by scanning and transmission electron microscope, N2 adsorption experiment, X-ray diffraction, Fourier transform infrared spectroscopy and UV-Vis absorption spectra. The rattle type structure was conformed and the sphere-like structure with the average size of 70 nm and hexagonal wurtzite crystal structure were also observed. The measurement results of optical properties showed even though ZnO@C@SiO2 presented no photocatalysis, ZnO@void@SiO2 showed high activity even the ZnO core was encapsulated with the SiO2 hollow.


2016 ◽  
Vol 52 (16) ◽  
pp. 3434-3437 ◽  
Author(s):  
H. L. Hellstern ◽  
A. Mamakhel ◽  
M. Bremholm ◽  
B. B. Iversen

A green, fast, high-throughput, continuous-flow hydrothermal synthesis method is explored for preparation of silica coated nanoparticles with narrow size distribution.


MRS Advances ◽  
2016 ◽  
Vol 1 (15) ◽  
pp. 1061-1066
Author(s):  
Dalaver H. Anjum ◽  
Shahid Rasul ◽  
Manuel A. Roldan-Gutierrez ◽  
Pedro M. F. J. Costa

ABSTRACTA nanoporous carbon (C) material, functionalized with Cobalt-Oxide/Cobalt (CoO/Co) core-shell nanoparticles (NPs), was structurally and chemically characterized with transmission electron microcopy (TEM) while its electrochemical response for Lithium ion battery (LIB) applications was evaluated as well. The results herein show that the nanoporous C material was uniformly functionalized with the CoO/Co core-shell NPs. Further the NPs were crystalline with fcc-type lattice on the Co2+ oxide shell and hcp-type core of metallic Co0. The electrochemical study was carried out by using galvanostatic charge/discharge cycling at a current density of 1000 mA g−1. The potential of this hybrid material for LIB applications was confirmed and it is attributed to the successful dispersion of the Co2+/ Co0 NPs in the C support.


2004 ◽  
Vol 818 ◽  
Author(s):  
Zhihui Ban ◽  
C. J. O'Connor

AbstractA homogeneous non-aqueous solution reactions method has been developed to prepare gold-coated cobalt (Co@Au) nanoparticles. After the sample was washed with 8% HCl, XRD (X-Ray Diffraction), TEM (transmission electron microscopy), and magnetic measurements SQUID (Superconducting Quantum Interference Device) are utilized to characterize the nanocomposites. XRD shows the pattern of sample, which is responding to gold and cobalt, no cobalt oxide was found. TEM results show that the average size of Co@Au nanoparticles is about 10 nm and we can find core-shell structure of the sample. SQUID results show that the particles are ferromagnetic materials at 300K. So the gold- coated cobalt nanoparticles (Co@Au) can be successfully prepared by the homogeneous nonaqueous approach. This kind of core-shell materials is stable in acid condition, which would give many opportunities for bio- application.


2018 ◽  
Vol 12 (1) ◽  
pp. 29-39 ◽  
Author(s):  
Navinchandra G. Shimpi ◽  
Mujahid Khan ◽  
Sharda Shirole ◽  
Shriram Sonawane

Objective:The present study is deals with the green synthesis of silver (AgNPs), iron oxide (α-Fe2O3NPs) and core-shell (Ag-α-Fe2O3CNPs) nanoparticles using the aqueous extract ofAlstonia scholariswithout any catalyst, template or surfactant or any intermediate under ultrasound cavitation technique. The purpose was to facilitate the high level of dispersion with increase in rate of reaction. Further AgNPs and α-Fe2O3NPs were used to synthesis Ag-Fe2O3CNPs in aqueous extract ofAlstonia scholarisunder controlled ultrasound cavitation technique.Methods:The size of AgNPs and Ag-Fe2O3CNPs can be tuned by optimizing various reaction parameters. UV-visible, X-ray diffraction spectroscopy (XRD), Transmission electron microscopy (TEM), Field emission scanning electron microscope (FE-SEM) and Fourier transform infra-red spectroscopy has been used for the characterization of silver and core shell Ag@Fe2O3nanoparticles. TEM images clearly show the formation of core shell nanoparticles with spherical morphology.Result:Fourier transform infra-red spectroscopy analysis revealed that carbohydrate, polyphenols, and protein molecules were involved in the synthesis and capping of silver, iron oxide and Ag@Fe2O3CNPs.


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